Enantioselective and enantiospecific transition-metal-catalyzed cross-coupling reactions of organometallic reagents to construct C–C bonds

AH Cherney, NT Kadunce, SE Reisman - Chemical Reviews, 2015 - ACS Publications
The stereocontrolled construction of C− C bonds remains one of the foremost challenges in
organic synthesis. At the heart of any chemical synthesis of a natural product or designed …

Recent advances in homogeneous nickel catalysis

SZ Tasker, EA Standley, TF Jamison - Nature, 2014 - nature.com
Tremendous advances have been made in nickel catalysis over the past decade. Several
key properties of nickel, such as facile oxidative addition and ready access to multiple …

Exploration of earth-abundant transition metals (Fe, Co, and Ni) as catalysts in unreactive chemical bond activations

B Su, ZC Cao, ZJ Shi - Accounts of chemical research, 2015 - ACS Publications
Conspectus Activation of inert chemical bonds, such as C–H, C–O, C–C, and so on, is a very
important area, to which has been drawn much attention by chemists for a long time and …

Breaking amides using nickel catalysis

JE Dander, NK Garg - ACS catalysis, 2017 - ACS Publications
Amides have been widely studied for decades, but their synthetic utility has remained limited
in reactions that proceed with rupture of the amide C–N bond. Using Ni catalysis, we have …

Activation of C–O and C–N bonds using non-precious-metal catalysis

TB Boit, AS Bulger, JE Dander, NK Garg - ACS catalysis, 2020 - ACS Publications
Metal-catalyzed cross-couplings represent one of the most important reaction platforms in
modern synthetic chemistry (Figure 1 A). 1 Although the field enjoys a rich history, there …

Dynamic kinetic cross-electrophile arylation of benzyl alcohols by nickel catalysis

P Guo, K Wang, WJ Jin, H Xie, L Qi… - Journal of the …, 2020 - ACS Publications
Catalytic transformation of alcohols via metal-catalyzed cross-coupling reactions is very
important, but it typically relies on a multistep procedure. We here report a dynamic kinetic …

Enantioselective benzylic C–H arylation via photoredox and nickel dual catalysis

X Cheng, H Lu, Z Lu - Nature Communications, 2019 - nature.com
The asymmetric cross-coupling reaction is developed as a straightforward strategy toward 1,
1-diaryl alkanes, which are a key skeleton in a series of natural products and bioactive …

Nickel-catalyzed asymmetric reductive cross-coupling to access 1, 1-diarylalkanes

KE Poremba, NT Kadunce, N Suzuki… - Journal of the …, 2017 - ACS Publications
An asymmetric Ni-catalyzed reductive cross-coupling of (hetero) aryl iodides and benzylic
chlorides has been developed to prepare enantioenriched 1, 1-diarylalkanes. As part of …

Enantiospecific sp2sp3 coupling of secondary and tertiary boronic esters

A Bonet, M Odachowski, D Leonori, S Essafi… - Nature …, 2014 - nature.com
The cross-coupling of boronic acids and related derivatives with sp 2 electrophiles (the
Suzuki–Miyaura reaction) is one of the most powerful C–C bond formation reactions in …

Alcohols as Latent Coupling Fragments for Metallaphotoredox Catalysis: sp3–sp2 Cross-Coupling of Oxalates with Aryl Halides

X Zhang, DWC MacMillan - Journal of the American Chemical …, 2016 - ACS Publications
Alkyl oxalates, prepared from their corresponding alcohols, are engaged for the first time as
carbon radical fragments in metallaphotoredox catalysis. In this report, we demonstrate that …